Ultrafast nonlinear absorption with multiple transformations and transient dynamics of gold nanobipyramids.

The process and condition of saturable absorption (SA) and reverse saturable absorption (RSA) of ultrafast nonlinear optics in metal nanoparticles are essential for applications including light generation, amplification, modulation, and switching. Here, we first discover and explore the multiple transformations (SA-RSA-SA) of ultrafast nonlinear absorption behavior of metal nanoparticles in femtosecond pulses. Correspondingly, the energy level model and fitting formula of multiple transformations are established to illustrate the process of optical response. The femtosecond transient absorption spectra provide information about their ultrafast dynamics process and vibrational mode, which further reveals the multiple transformation mechanisms of nonlinear absorption in gold nanobipyramids (Au-NBPs). Furthermore, Au-NBPs exhibit a significantly higher SA modulation depth up to 42% in the femtosecond, which is much higher than the reported values of other nanomaterials. Our results indicate that Au-NBPs can be used as broadband ultrafast Q-switching and mode-locking, and the conversion offers new opportunities for metal nanostructures in applications of optical switching.

D-π-A type conjugated indandione derivatives: ultrafast broadband nonlinear absorption responses and transient dynamics.

The ultrafast nonlinear optical response of two 1,3-indandione derivatives (INB3 and INT3) was systematically investigated by the femtosecond Z-scan and pump-probe technique at multiple visible and near infrared wavelengths. Both compounds show strong broadband nonlinear absorption (NLA) and different wavelength-dependent two-photon absorption (TPA) characteristics in the range of 650-1100 nm. The TPA cross section of trithiophene-based compound INT3 was found to be larger than that of triphenylamine-based compound INB3 in the red region (650-800 nm), which is attributed to its longer π-conjugated structure and better molecular planarity. Interestingly, the effective NLA of INB3 was found to be larger than INT3 in the NIR region (800-1100 nm), which is related to the excited state absorption (ESA) induced by TPA. The ultrafast dynamics of both compounds were investigated by femtosecond transient absorption spectroscopy, which revealed a broadband ESA including several relaxation processes. This work extends nonlinear optical research on indandione derivatives, and the results suggest that these derivatives are promising candidates for optical limiting applications.

Correction: D-π-A type conjugated indandione derivatives: ultrafast broadband nonlinear absorption responses and transient dynamics.

[This corrects the article DOI: 10.1039/D2RA00349J.].

Nonlinear optical properties of InP/ZnS core-shell quantum dots.

The nonlinear optical properties of an InP/ZnS core-shell quantum dot toluene solution were investigated using a Z-scan and transient absorption technique with femtosecond pulses and nanosecond pulses at 532 nm wavelengths, respectively. The research results showed that InP/ZnS core-shell quantum dots exhibited saturated absorption under the excitation of femtosecond pulses, and the switch from saturated absorption to reverse saturated absorption was observed under the excitation of nanosecond pulses. The mechanism of the switch was attributed to excited-state absorption. Moreover, the nonlinear refraction was shown as self-focusing and self-defocusing under the excitation of femtosecond and nanosecond pulses, respectively, which were attributed to the Kerr effect of electrons and the thermal effect of InP/ZnS quantum dots, respectively. The investigations show that InP/ZnS core-shell quantum dots are good materials, and have many potential applications in optical and electrical fields.

Wavelength-dependent nonlinear absorption and ultrafast dynamics process of Au triangular nanoprisms.

The nonlinear absorption and ultrafast dynamics process of Au triangular nanoprisms were investigated by using broadband (ranging from 550 to 700 nm) nanosecond Z-scan measurements and femtosecond time-resolved transient absorption spectrum, respectively. We found that Au triangular nanoprisms exhibit saturation absorption (SA) at low excitation intensities. With the increase of incident intensity, a switch from SA to reverse saturation absorption (RSA) occurs. Photo-dynamics process was found to be a double-exponential energy relaxation with a fast and a slow decay component. Interestingly, when probe wavelength is away from the plasma resonance peak, the decay of relaxation also shows the modulation due to the vibration mode of the coherent excitation.